Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507520
PTPN11
0.658 0.520 12 112453279 missense variant G/C;T snv 39
rs80338796
RAF1
0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 37
rs121918457
PTPN11
0.701 0.280 12 112488466 missense variant C/T snv 4.0E-06 7.0E-06 24
rs121918456
PTPN11
0.752 0.280 12 112473023 missense variant A/C;G snv 13
rs397507549
PTPN11
0.742 0.240 12 112489104 missense variant C/A;G snv 13
rs121918470
PTPN11
0.790 0.160 12 112489105 missense variant A/C;G snv 4.0E-06 10
rs397507542
PTPN11
0.790 0.320 12 112489069 missense variant G/T snv 9
rs80338797
RAF1
0.827 0.160 3 12584624 missense variant G/C;T snv 7
rs387906661
BRAF
0.807 0.280 7 140801551 missense variant T/G snv 6
rs397507466
BRAF
0.807 0.280 7 140801537 missense variant T/A;C;G snv 4.0E-06 6
rs397507548
PTPN11
0.851 0.160 12 112489093 missense variant A/C snv 6
rs587782360
PTEN
0.851 0.280 10 87933162 missense variant A/G snv 5
rs397507529
PTPN11
0.851 0.160 12 112473031 missense variant A/G snv 7.0E-06 5
rs397507541
PTPN11
0.827 0.160 12 112489068 missense variant C/T snv 4.0E-06 7.0E-06 5
rs397509345
PTPN11
0.851 0.160 12 112489093 missense variant AG/CC mnv 5
rs587782343
PTEN
0.851 0.200 10 87933073 missense variant G/A snv 4
rs121918468
PTPN11
0.882 0.160 12 112488444 missense variant G/A;T snv 3
rs121918469
PTPN11
0.882 0.160 12 112488454 missense variant G/C snv 3
rs397507523
PTPN11
0.882 0.160 12 112472954 missense variant A/G snv 3
rs397507550
PTPN11
0.882 0.160 12 112489106 missense variant G/A;C snv 3
rs80338799
RAF1
0.882 0.160 3 12585745 missense variant G/A;C snv 3
rs80338798
RAF1
0.925 0.160 3 12585761 missense variant C/T snv 2
rs190222208
SOS1
0.925 0.160 2 39035268 missense variant G/A snv 8.0E-05 8.4E-05 2
rs765467335
ACP1
1.000 0.160 2 277247 missense variant G/T snv 1.2E-05 1
rs753025128
PIK3CD
1.000 0.160 1 9720755 missense variant G/A snv 8.1E-06 7.0E-06 1